4.3 Article

Zirconium(IV) chloride-mediated chemoselective conjugate addition of aliphatic amines to alpha,beta-ethylenic compounds

Journal

SYNTHETIC COMMUNICATIONS
Volume 36, Issue 6, Pages 795-801

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/00397910500451423

Keywords

amines; Michael addition; alpha,beta-unsaturated compounds; zirconium(IV) chloride

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Zirconium chloride efficiently catalyzes the conjugate addition of a variety of aliphatic amines to alpha,ss-unsaturated ester, nitriles, and ketones to give the corresponding ss-amino derivatives in excellent yields under mild reaction conditions. Aromatic amines do not participate in this transformation.

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